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Chemistry for engineering solutions Silvia Bodoardo 1
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• definition
• solubility
• concentration
•colligative properties
• elettrolites
colligative properties
CONTENTSCONTENTS
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SOLUTIONSSOLUTIONS
A solution is an homogenous mixture of atoms, molecules or
ions distributed in the whole space.
The most abundant component is the solvent: solutes dissolve in
solvents
Gas mixtures
liquid solutions
solid solutions
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SOLUBILITYSOLUBILITY
similia similibus solvuntur
When the bonds in the solute and in the solvent are of the same
nature, solubility is possible
when excess undissolved solute is in dinamic equilibrium with
the dissolved solute, the solution is called saturated.
Solubility depens on Kps (v.)
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+ + +
+ +
+++ -
--
--
-
-
SOLVATAZIONESOLVATAZIONE
+
-
For ionic compounds, when ions are surronded by solvent
molecules adequately oriented, ions become solvated.
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metanole solubility in water
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DISSOLUTION OF SOLUTESDISSOLUTION OF SOLUTES
For ionic compounds, when ions are surronded by solvent
molecules adequately oriented, ions become solvated..
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ExamplesExamples of of solventsolvent--solutessolutes interactioninteraction
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quantitative quantitative waysways of of expressingexpressing the the
concentrationconcentration of a of a solutionsolution
mass percent: g solute in 100 g solution
volume percent: ml solute in 100 ml solution
MOLARITY (M): solute moles in 1 liter solution
MOLALITY (m): solute moles in 1000 g solvent
mole fraction: χs = n/(n+N) ; n = solute moles;
N = solvent moles
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ColligativeColligative propertiesproperties
Some properties of the solution depend on the amount of
the solute and of the solvent and are indipendent by the
type of solute.
These properties are called colligative properties.
The most important colligative properties are:
• vapour presure lowering
• boiling point elevation
• freezing point depression
• osmotic pressure
Laws regulating colligative properties are different for
electrolyte and non electrolyte
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VapourVapour pressurepressure of of solutionssolutions
Raoult law (solid solute, liquid solvent):
(p° - P)/p° = n/n+N
The vapour pressure of a solution, in the same experimental
conditions, are always lower than the one of the pure
solvent.
P: total vap. pres.
p°:solvent vap. pres.
n: solute moles
N: solvent moles
According to Raoult, the vapour pressure of a solvent is
proportional to its mole fraction in the solution
It can be used only for ideal solutions
(Raoult solutions)
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Ideal solution:
the solution is diluited
The vapor pressure of the solute is
negligible respect to that of the solvent
the solute does not bond to the
solute and does not dissociate
The solute does not react with
the solvent
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BoilingBoiling pointpoint elevationelevation: ∆Teb = keb m
FreezingFreezing pointpoint depressiondepression : ∆Tcr = kcr m
∆Teb = (p°/k). m ; keb = (p°/k)
∆Teb = keb m
Characteristic of the sole solvent
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osmoticosmotic pressurepressure
π V = n RT
The osmotic pressure depends on the
Volume and the absolute Temperature,
according to Van’t Hoff equation
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ELETTROLYTES SOLUTIONSELETTROLYTES SOLUTIONS
Some substances (salts, acides, bases) dissociates in solution
producing ions.
Examples: KCl K+(aq) + Cl-(aq)
H2SO4 2H+(aq) + SO4--(aq)
KOH K+(aq) + OH-(aq)
Elettrolytic solutions
They are called electrolytes
(strong complete dissociation)
(weak partial dissociation)
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The amount of the dissocation is measured by the
dissociation degree α:
Dissociation degree α = Ndiss/N
Dissociated moles Ndiss = α N
Undissociated moles Nind = N - α N
Produced ions z α N
particles in solution N - α N + z α N = N (1 - α (z - 1))
i - 1α = ------
z - 1
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For electrolytes solutions, it is sufficient to add the Van’t Hoff
coefficient i in the described expressions :
i = 1 + α (z-1)
α = dissociation degree
z = number of produced ions
P = p° - p°(n i/ (n i + N))
∆Teb = keb m i
∆Tcr = kcr m i
π V = n i RT
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